Product recall
Recalled by Shaman Botanicals, LLC
The product, as the FDA describes it: Product label reads in part as "WHITE VEIN ADVANCED ALKALOIDS CHEWABLE TABLETS 15mg 7-Hydroxymitragynine per container (7.5mg 7-OH per serving) LEMON DIETARY SUPPLEMENT Net Wt. 0.02 oz 2 TABLETS Supplement Facts 7-hydroxymitragynine 7.5 mg MANUFACTURED BY: Konig Products, LLC 30 N Gould Street, Suite R, Sheridan, WY 82801"; Packaging: Sealed silver metallic bag with a front and back sticker for the labels; Product label reads in part as "WHITE VEIN ADVANCED ALKALOIDS CHEWABLE TABLETS 150mg total 7-Hydroxymitragynine per container (10 Packets x 2 Tablets Each) 7.5mg 7-OH per tablet/serving, LEMON DIETARY SUPPLEMENT Net Wt. 0.17 oz 10 PACKETS 2 TABLETS EACH Supplement Facts 7-hydroxymitragynine 7.5 mg MANUFACTURED BY: Konig Products, LLC 30 N Gould Street, Suite R, Sheridan, WY 82801"; Packaging: Sealed black flexible plastic bag with multi color sticker label on front and back UPC 810057763724
Why it was recalled
A sample of the product had the active ingredient in a quantity greater than the labeled specification.
What to do if you have it
The food itself is not the problem here. What is on the package does not match what is inside, which matters most for anyone counting on the label, whether that is an allergy, a medical diet, or feeding a small child. Check the official notice for what the correct product should have said.
How to tell whether your package is one of them
A recall covers particular production runs, not everything the company makes, so the codes decide it. These are the ones the FDA published. Match them against what is printed on your package, usually near the best-before date.
B#AAW.501.3; all expiration dates
The details on record
| Recalling company | Shaman Botanicals, LLC |
|---|---|
| Company location | North Kansas City, MO |
| Where it was distributed | Firm has provided the following information: 14 wholesalers, 108 Distributors, 46 Company-owned stores, 2202 online customers |
| How much was recalled | 2 pack: 1281 units; 20-count: 14,491 units |
| Recall started | February 13, 2026 |
| Published by the FDA | March 25, 2026 |
| Recall type | Voluntary: Firm initiated |
| How the company announced it | Press Release |
| FDA recall number | H-1107-2026 |
Everything above comes from the FDA enforcement report for this recall. Read the official notice for the company's own wording, contact numbers, and any photographs of the packaging.
The other half of the answer
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